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. 2023 Jun 22;23(2):570–578. doi: 10.1007/s12311-023-01578-6

Table 1.

Demographic and clinical features of included patients

Patient Age, y Age at onset, y Disease duration, y Sex Diagnosis SARA ICARS
1 42 35 7 M SCA1 6 15
2 50 40 10 F SCA1 3 7
3 28 7 21 F AOA2 21 52
4 44 36 8 M SCA1 11.5 29
5 49 43 6 F SAOA 9 23
6 34 32 2 F SAOA 5 9
7 42 41 1 M SAOA 4 13
8 51 47 4 F SAOA 8 18
9 44 39 5 F SCA2 12 28
10 55 49 6 F SAOA 3 11
11 23 20 3 F SCA2 14 38
12 70 68 2 M MSA-C 12 23
13 59 57 2 F SAOA 13.5 26
14 68 45 23 F SCA38 16 38
15 56 54 2 F SCA2 4 13
16 73 61 12 F MSA-C 10 21
17 59 50 9 M SCA2 7 16
18 59 57 2 M SAOA 12 27
19 48 45 3 M SAOA 13 38
20 42 35 7 M SCA1 8 19
21 58 46 12 M SCA2 12 28
22 80 71 9 M SAOA 5 12
23 68 64 4 F SAOA 4.5 8
24 65 61 4 F SAOA 3 6
25 39 34 5 M SCA1 9 17
26 59 50 9 F SAOA 10 21

SCA spinocerebellar ataxia, AOA2 ataxia with oculomotor apraxia type 2, MSA-C cerebellar variant of multiple system atrophy, SAOA sporadic adult-onset ataxia, SARA Scale for the Assessment and Rating of Ataxia, ICARS International Cooperative Ataxia Rating Scale, M male, F female, y years